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[Aortic Intramural Hematoma: a Challenging Diagnosis]
Bernhard Haring1, Ralph Kickuth2, Friederika Fluck2
1Medizinische Klinik und Poliklinik I, Universitätsklinikum Würzburg.
Deutsche Medizinische Wochenschrift (1946)
|March 30, 2019
Summary
A 75-year-old woman with acute abdominal pain was diagnosed with intramural hematoma of the aorta. Endovascular repair was successful for her complicated Stanford Type B aortic syndrome, leading to recovery.
Area of Science:
- Cardiovascular Medicine
- Vascular Surgery
- Diagnostic Imaging
Background:
- Acute aortic syndrome (AAS) encompasses life-threatening conditions like aortic dissection, intramural hematoma (IMH), and penetrating atherosclerotic ulcers.
- Prompt diagnosis and management are critical for AAS, with differing treatment strategies for Stanford Type A and Type B classifications.
Observation:
- A 75-year-old female presented with acute abdominal pain, a history of cardiovascular conditions, and was on apixaban.
- Imaging revealed an intramural hematoma of the aorta extending from the left subclavian to the inferior mesenteric artery, with ulcer-like projections.
Findings:
- Initial conservative management with blood pressure control for the descending aortic intramural hematoma was unsuccessful.
- The patient underwent successful endovascular aortic repair (TEVAR) for complicated Stanford Type B aortic syndrome.
- The patient experienced a good recovery and was discharged.
Implications:
- Endovascular aortic repair is a viable option for complicated Stanford Type B aortic intramural hematoma when conservative measures fail.
- Timely and accurate diagnosis of AAS is crucial for effective treatment planning.
- This case highlights the importance of considering advanced interventions for aortic pathologies presenting with persistent symptoms.
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